I'm looking for...
close

Did you know that your Internet Explorer is out of date?

To get the best possible experience using our website we recommend that you upgrade to a newer version or download another web browser.
A list of the most popular web browsers can be found below. Just click on the icons to get to the download page.

crome
Google Chrome
IE
Internet Explorer
firefox
Mozilla Firefox
opera
Opera

Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Contact Info
Angela McCauley
Life Science

+353 87 696 0951
[email protected]
Connect with me on
Operations Lead
Dublin South
R&D Director
Galway
Project Manager
Limerick
R&D Director
Galway
CQV Lead
Tipperary
Senior R&D Engineer
Galway City
Project Engineer
Tipperary
Project Engineer
Republic of Ireland
R&D Engineer
Dublin
Project Engineer
Limerick
R&D Manager
Galway
Trainer
Dublin
Chemical Engineer
Tipperary
Senior Manufacting Engineer
Republic of Ireland
R&D Manager
Galway
Senior Recruitment Consultant
Republic of Ireland
Analytical Chemist
Tipperary
R&D Director
Galway
R&D Manager
Galway
Responsible Person (RP)
Republic of Ireland
Project Engineer
Limerick
Senior Quality Engineer-Remote
Republic of Ireland
Process Engineer
Limerick
Recruitment Consultant
Republic of Ireland
Head of R&D
Galway
Senior Recruitment Consultant
Republic of Ireland
R&D Manager
Galway
Medical Device Director
Republic of Ireland
C&Q Lead
Tipperary
Quality Specialist
Tipperary
Apply for this job

Name:

Surname:

Email:

Phone:

Cv:

Salary Expectations:

Education:

Experience:

Current Location:

Notice Period:

Write here your cover note:


If you would like us to create a jobseeker account for you, giving you access to
account management, job alerts and one-click applications, then please tick this box

If you are having difficulty you can always email your cv to [email protected]
Details

Senior QC Associate


Reference:AMC1234 Location: Dublin
Dublin South
Qualification:DegreeExperience:2-3 Years
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: QC Analyst

AMC1234
Senior QC Associate
Contract – 12 months
Dublin
Senior QC Associate


Would you like to join a leading and biopharmaceutical company in Dublin, to further develop your career? This is an excellent opportunity to work on leading technologies in the biotech industry. As a QC Senior Associate, you willbe responsible for planning, executing and documenting the qualification, calibration and routine maintenance of laboratory systems for cGMP Quality Control laboratory facilities.

To be successful in this role you must have a minimum of 3 years laboratory experience in cGMP laboratory environment including exposure to analytical instrument validation experience.


Responsibilities

  • Managing & coordinating the schedules of Calibration Technicians & ensuring that all maintenance & calibration activities are tracked & managed through the Computerised Maintenance Management System (CMMS)
  • Authoring/owning and approving Validation Life Cycle documents for computer related systems including responsibility for Data Integrity testing and business administration of Laboratory Computer Related systems.
  • Commissioning of new laboratory equipment and facilities including developing lab equipment specifications
  • Writing equipment validation protocols and associated summary reports.
  • Conduct periodic reviews of instrument validation as part of validation life cycle.
  • Act as a subject matter expert on instrument validation regulations and procedures.
  • Serving as the point of contact with laboratory equipment vendors and engineers
  • Coordination of equipment repairs and maintenance with vendors/contractors and also carrying out equipment maintenance as required.
  • Writing/contributing to equipment operating procedures and manuals.
  • Designing and conducting training for QC staff, and other department staff as applicable
  • Project manage Change controls and adhere to Change Control metrics.
  • Periodic management updates on activities to senior management.
  • Planning and conducting routine calibration, requalification and maintenance of laboratory equipment and ensure calibration and maintenance schedules are adhered to.

What you need:
  • Minimum of 3 years of laboratory experience in a cGMP laboratory environment including exposure to analytical instrument validation.
  • Knowledge of the methodology and instrumentation and analytical techniques used for biopharmaceutical testing.
  • Understanding of current regulatory requirements for cGMP laboratory equipment validation and electronic record integrity.
  • Demonstrated success in managing an equipment qualification or maintenance program advantageous.
If you meet the minimum requirements, and feel this is the right role for you, please apply today!


For further details please contact Angela McCauley on 00 353 (0)876930951 or send CV in confidence to [email protected]